Recalls / —
—#84110
Product
Zimmer VerSys Hip System Femoral Head, 12/14 taper, 28 mm dia., neck length +0 mm, sterile, Zimmer, Warsaw, IN; REF 8018-28-02. Intended for mating femoral stems equipped with tapered necks.
- FDA product code
- LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- Device class
- Class 2
- Medical specialty
- Orthopedic
- 510(k) numbers
- K953337
- Affected lot / code info
- Lot 60378581.
Why it was recalled
Manufacturing material may be present on the surface of the implant.
Root cause (FDA determination)
Manufacturing material removal
Action the firm took
An Urgent: Device Recall letter, dated 8/3/2009, was issued to consignees. The letter identified the affected product, stated the reason for the recall, the clinical implications (risks to health), and actions to be taken. Customers are to locate any unused devices and quarantine them immediately, carry out a physical count of affected product and record the data on the Return Certification Form included with the letter, and fax a copy of the completed form back to Zimmer, Inc. at 574-372-4265. Customers are to return the recalled product along with the completed Inventory Return Certification Form. A "Dear Surgeon" letter will be issued to any hospitals where the devices have been implanted.
Recalling firm
- Firm
- Zimmer Inc.
- Address
- 345 E Main St, Warsaw, Indiana 46580-2746
Distribution
- Distribution pattern
- Worldwide Distribution -- USA, Brazil, Canada, and Switzerland.
Timeline
- Recall initiated
- 2009-08-03
- Posted by FDA
- 2009-11-13
- Terminated
- 2009-12-15
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #84110. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.